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Variant : CV700337 (NM_177531.6(PKHD1L1):c.2870C>A (p.Ala957Glu)) Homo sapiens

Symbol: CV700337
Name: NM_177531.6(PKHD1L1):c.2870C>A (p.Ala957Glu)
Condition: not provided [RCV000956658]
Clinical Significance: benign
Last Evaluated: 04/10/2018
Review Status: criteria provided, single submitter
Related Genes: PKHD1L1  
Variant Type: single nucleotide variant (SO:0001583)
Source: CLINVAR
Molecular Consequence: missense variant
Evidence: clinical testing
HGVS Name(s): NM_177531.6:c.2870C>A
NC_000008.11:g.109427026C>A
NC_000008.10:g.110439255C>A
NM_177531.4:c.2870C>A
NP_803875.2:p.Ala957Glu
Position
Human AssemblyChrPosition (strand)Source
GRCh388109,427,026 - 109,427,026CLINVAR
GRCh378110,439,255 - 110,439,255CLINVAR
Cytogenetic Map88q23.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 15198121
Created: 2020-01-07
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.